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Results 1 - 10 of 23 for Uniparental heterodisomy
  1. Genomic imprinting and uniparental disomy are factors that influence how some genetic conditions are inherited. People usually inherit two copies of each gene—one ...
  2. GeneReviews Glossary From the National Institutes of Health (National Center for Biotechnology Information)  
    Newborn Screening/Reference Desk ... Newborn Screening ... Genetic Testing/Reference Desk ... Genetic Testing ... National Center for Biotechnology Information ... From the National ...
  3. Prader-Willi Syndrome (PWS): Other FAQs From the National Institutes of Health (Eunice Kennedy Shriver National Institute of Child Health and Human Development)  
    Prader-Willi Syndrome/Learn More ... Prader-Willi Syndrome ... Eunice Kennedy Shriver National Institute of Child Health and Human Development ... From the National ...
  4. ... can also result from a chromosome abnormality called uniparental disomy (UPD). UPD occurs when people inherit both copies ... CA, Bass NE, Zinn AB, Schwartz S. Maternal uniparental disomy chromosome 14: case report and literature review. Pediatr ...
  5. ... from each parent. This situation is called maternal uniparental disomy. Rarely, Prader-Willi syndrome can also be caused ... in the paternal chromosome 15 or by maternal uniparental disomy. These genetic changes occur as random events during ...
  6. ... from each parent. This phenomenon is called paternal uniparental disomy. Rarely, Angelman syndrome can also be caused by ... in the maternal chromosome 15 or by paternal uniparental disomy. These genetic changes occur as random events during ...
  7. ... caused by a genetic change known as paternal uniparental disomy (UPD) of chromosome 6. In paternal UPD, people ... are not inherited, particularly those caused by paternal uniparental disomy. In these cases, genetic changes occur as random ...
  8. ... caused by a genetic change known as paternal uniparental disomy (UPD). Paternal UPD causes people to have two ... R, Macdonald F, Maher ER. Mitotic recombination and uniparental disomy in Beckwith-Wiedemann syndrome. Genomics. 2007 May;89( ...
  9. What is Prader-Willi Syndrome? (Prader-Willi Syndrome Association)  
    Prader-Willi Syndrome (PWS) is a rare genetic disorder characterized by chronic hunger, growth hormone deficiency, and behavior challenges. ... Prader-Willi ...
  10. ... mean by anticipation? What are genomic imprinting and uniparental disomy? Are chromosomal disorders inherited? Why are some genetic ...
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